Dietary Inulin to Improve SARS-CoV-2 Vaccine Response in Kidney Transplant Recipients: The RIVASTIM-Inulin Randomised Controlled Trial

Author:

Singer Julian12ORCID,Tunbridge Matthew J.3,Shi Bree2,Perkins Griffith B.45ORCID,Chai Cheng Sheng4,Salehi Tania3,Sim Beatrice Z.3,Kireta Svjetlana3,Johnston Julie K.3,Akerman Anouschka6ORCID,Milogiannakis Vanessa6,Aggarwal Anupriya6ORCID,Turville Stuart6,Hissaria Pravin47,Ying Tracey12,Wu Huiling12,Grubor-Bauk Branka48ORCID,Coates P. Toby34,Chadban Steven J.12ORCID

Affiliation:

1. Department of Renal Medicine, Royal Prince Alfred Hospital, Sydney, NSW 2050, Australia

2. Central Clinical School, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2006, Australia

3. Central and Northern Adelaide Renal and Transplantation Service, Royal Adelaide Hospital, Adelaide, SA 5000, Australia

4. Adelaide Medical School, University of Adelaide, Adelaide, SA 5000, Australia

5. Immunology Directorate, SA Pathology, Adelaide, SA 5000, Australia

6. Kirby Institute, University of New South Wales, Sydney, NSW 2052, Australia

7. Department of Immunology and Allergy, Royal Adelaide Hospital, Adelaide, SA 5000, Australia

8. Viral Immunology Group, Basil Hetzel Institute for Translational Health Research, University of Adelaide, Adelaide, SA 5011, Australia

Abstract

Kidney transplant recipients are at an increased risk of hospitalisation and death from SARS-CoV-2 infection, and standard two-dose vaccination schedules are typically inadequate to generate protective immunity. Gut dysbiosis, which is common among kidney transplant recipients and known to effect systemic immunity, may be a contributing factor to a lack of vaccine immunogenicity in this at-risk cohort. The gut microbiota modulates vaccine responses, with the production of immunomodulatory short-chain fatty acids by bacteria such as Bifidobacterium associated with heightened vaccine responses in both observational and experimental studies. As SCFA-producing populations in the gut microbiota are enhanced by diets rich in non-digestible fibre, dietary supplementation with prebiotic fibre emerges as a potential adjuvant strategy to correct dysbiosis and improve vaccine-induced immunity. In a randomised, double-bind, placebo-controlled trial of 72 kidney transplant recipients, we found dietary supplementation with prebiotic inulin for 4 weeks before and after a third SARS-CoV2 mRNA vaccine to be feasible, tolerable, and safe. Inulin supplementation resulted in an increase in gut Bifidobacterium, as determined by 16S RNA sequencing, but did not increase in vitro neutralisation of live SARS-CoV-2 virus at 4 weeks following a third vaccination. Dietary fibre supplementation is a feasible strategy with the potential to enhance vaccine-induced immunity and warrants further investigation.

Publisher

MDPI AG

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